{{Rsnum
|rsid=6746082
|Gene=DTNB
|Chromosome=2
|position=25436375
|Orientation=plus
|GMAF=0.405
|Gene_s=DTNB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 56.6 | 37.2 | 6.2
| HCB | 8.0 | 48.9 | 43.1
| JPT | 9.7 | 50.4 | 39.8
| YRI | 19.7 | 49.7 | 30.6
| ASW | 19.3 | 63.2 | 17.5
| CHB | 8.0 | 48.9 | 43.1
| CHD | 15.7 | 50.0 | 34.3
| GIH | 63.4 | 32.7 | 4.0
| LWK | 27.3 | 46.4 | 26.4
| MEX | 54.4 | 40.4 | 5.3
| MKK | 37.4 | 52.3 | 10.3
| TSI | 70.6 | 25.5 | 3.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22120009
|Trait=None
|Title=Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
|RiskAllele=A
|Pval=4E-7
|OR=1.2900
|ORtxt=None
}}

{{PMID Auto
|PMID=24449210
|Title=Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}